Mutation Analysis of 17α-Hydroxylase
NCT00172510 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 25
Last updated 2005-09-15
Summary
To elucidate the molecular pathology of the 4 families with 17α-hydroxylase/17,20-lyase deficiency.
Conditions
- Pseudohermaphroditism
- Congenital Adrenal Hyperplasia
- Hypertension
Interventions
- PROCEDURE
-
blood drawing
Sponsors & Collaborators
-
National Taiwan University Hospital
lead OTHER
Principal Investigators
-
Yi-Ching Tung, MD · National Taiwan University Hospital
Eligibility
- Min Age
- 0 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-08-31
- Completion
- 2005-08-31
Countries
- Taiwan
Study Locations
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